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Job Description & How to Apply Below
The role, reporting to the Group Standards Compliance Manager, involves leading the design quality function, proactively offering and supporting improvements, and coordinating actions to help ensure precision and adherence to all quality design processes. The role includes championing a culture of quality, ensuring this reflects state of the art and contributing to the continued success and growth of the company. The successful candidate will work as part of a team developing new respiratory care products and supporting existing products.
Working in a busy and evolving environment, the successful candidate will have interactions throughout the business.
- Experience with in a design quality environment
- Experience working with technical documentation and data management
- Experience with in the medical device industry, with knowledge of EU MDR (2017/745) and ISO 13485, Excellent technical reading comprehension
- High levels of attention to detail
- Able to function in a highly regulated environment with a focus on quality
- Organised, efficient and strong administration skills
- Have a can-do attitude with an enthusiastic approach
- Good people skills and excellent communication
- Excellent verbal and written communication skills
- I.T. Literate - Microsoft Office
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